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Disease Info Card
Ovarian Hyperstimulation Syndrome
Information about Ovarian Hyperstimulation Syndrome: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Ovarian Hyperstimulation Syndrome
Most recent studies have shown that Ovarian Hyperstimulation Syndrome shares some biological mechanisms with anovulation, anovulatory-cycle, ectopic-pregnancy, endometrial-polyp, female-infertility, infertility, multiple-pregnancy, ovarian-cysts, ovarian-diseases, pain, pituitary-diseases, pleural-effusion-disorder, polycystic-ovary-syndrome, pregnancy-complications, subfertility, thrombosis, venous-thrombosis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Ovarian Hyperstimulation Syndrome, and have been seen in publications frequently: Angiogenesis, Blastocyst Development, Coagulation, Diuresis, Embryo Development, Embryo Implantation, Excretion, Fertilization, Hatching, Insemination, Luteinization, Luteolysis, Menstruation, Metaphase, Oocyte Maturation, Ovulation, Pathogenesis, Secretion, Transport, Vasodilation
Quite a number of genes have been found to play important roles in Ovarian Hyperstimulation Syndrome, such as AGRP, ALB, ART2B, BRD2, CGA, CYP19A1, DBT, FSHR, IL2, IL6, INS, PGR, PLOD1, PRL, REN, TMEM37, VEGFA. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.